Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs10914456 1.000 0.040 1 31622570 intron variant T/C snv 0.51 2
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs7973260 0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22